Mutations in B3GALNT2 cause congenital muscular dystrophy and hypoglycosylation of α-dystroglycan.

MLA

Stevens, Elizabeth, et al. “Mutations in B3GALNT2 Cause Congenital Muscular Dystrophy and Hypoglycosylation of α-Dystroglycan.” American Journal of Human Genetics, vol. 92, no. 3, Mar. 2013, pp. 354–65. EBSCOhost, https://doi.org/10.1016/j.ajhg.2013.01.016.

APA

Stevens, E., Carss, K. J., Cirak, S., Foley, A. R., Torelli, S., Willer, T., Tambunan, D. E., Yau, S., Brodd, L., Sewry, C. A., Feng, L., Haliloglu, G., Orhan, D., Dobyns, W. B., Enns, G. M., Manning, M., Krause, A., Salih, M. A., Walsh, C. A., … Muntoni, F. (2013). Mutations in B3GALNT2 cause congenital muscular dystrophy and hypoglycosylation of α-dystroglycan. American Journal of Human Genetics, 92(3), 354–365. https://doi.org/10.1016/j.ajhg.2013.01.016

Chicago

Stevens, Elizabeth, Keren J Carss, Sebahattin Cirak, A Reghan Foley, Silvia Torelli, Tobias Willer, Dimira E Tambunan, et al. 2013. “Mutations in B3GALNT2 Cause Congenital Muscular Dystrophy and Hypoglycosylation of α-Dystroglycan.” American Journal of Human Genetics 92 (3): 354–65. doi:10.1016/j.ajhg.2013.01.016.